A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5837



Internal ID15550686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:91769552..91772231hg38UCSC Ensembl
Outerchr7:91398867..91401546hg19UCSC Ensembl
Outerchr7:91236803..91239482hg18UCSC Ensembl
Outerchr7:91043518..91046197hg17UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg386416
hg196416
hg186416
hg176416
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2769
SamplesNA18555
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv5837
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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